EP0404794A1 - Atomic absorption spectrometer. - Google Patents
Atomic absorption spectrometer.Info
- Publication number
- EP0404794A1 EP0404794A1 EP89903130A EP89903130A EP0404794A1 EP 0404794 A1 EP0404794 A1 EP 0404794A1 EP 89903130 A EP89903130 A EP 89903130A EP 89903130 A EP89903130 A EP 89903130A EP 0404794 A1 EP0404794 A1 EP 0404794A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- light beam
- sample
- light source
- measuring light
- atomic absorption
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/3103—Atomic absorption analysis
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/3103—Atomic absorption analysis
- G01N2021/3111—Atomic absorption analysis using Zeeman split
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/256—Arrangements using two alternating lights and one detector
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/71—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light thermally excited
- G01N21/74—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light thermally excited using flameless atomising, e.g. graphite furnaces
Definitions
- the invention relates to an atomic absorption spectrometer containing
- Atomic absorption spectrometers are used to determine the amount or concentration of an element in a sample.
- a line of measurement light is directed from a line-emitting light source, for example a hollow cathode lamp, to a photoelectric detector.
- An atomizing device is arranged in the beam path of this measuring light bundle.
- the sample to be examined is atomized so that its components are in an atomic state.
- the measuring light bundle contains the resonance lines of the element sought. These resonance lines of the measuring light beam are absorbed by the atoms of the element sought in the atomic cloud, while ideally the other elements contained in the sample do not influence the measuring light beam.
- the measuring light beam is therefore weakened, which is a measure of the number of atoms of the element sought in the path of the measuring light beam and thus, depending on the atomization process used, a measure of the concentration or the amount of the element sought in the sample.
- the absorption that the measuring light beam experiences is not only caused by the atoms of the element sought.
- a flame, into which a sample is sprayed as a solution can serve as the atomizing device.
- the electrothermal atomization is preferably used: the sample is placed in an oven which is heated to a high temperature by passing electric current through it.
- the sample is first dried in the oven, then ashed and finally atomized.
- An "atomic cloud” then forms in the furnace, in which the element sought is present in atomic form.
- the measuring light beam is passed through this furnace.
- These ovens can have different shapes. They are usually made from graphite.
- a reference light bundle is passed through a flame or atomic cloud from a light source emitting a continuum with a wide bandwidth relative to the line width, the absorption of the measuring light bundle being caused by atomic absorption plus background absorption, while the absorption of the reference light beam is practically only determined by the background absorption.
- Another method for determining the background absorption is based on the Zeeman effect: by applying a magnetic field to the sample, the absorption lines of the element sought in the sample are shifted in relation to the spectral 1 in lines of the measuring beam, so that in the sample no atomic absorption takes place in the applied magnetic field and only the background absorption is measured. By switching the magnetic field on and off, the absorption corrected atomic absorption can be measured.
- the invention relates to an atomic absorption spectrometer in which the background absorption is determined by means of a reference light beam from a light source emitting a continuum.
- atomic absorption - spectrometer known in which a Messler i 'chtbündel originates from a line-emitting light source, and is passed through a flame or a furnace for the electrothermal atomization onto a detector, and in which alternately containing this a line spectrum of a looked-for element measuring light beam a reference light beam from a light source emitting a continuum takes effect.
- This reference light beam is reflected into the beam path of the measurement light beam by means of a beam splitter.
- the beam splitter is usually a partially transparent mirror.
- This mirror has evenly distributed reflecting and transmissive surface parts, so that 50% of the measurement light beam pass through the transmissive surface parts and 50% of the reference light beam is reflected on the reflecting surface parts in the direction of the measurement light bundle.
- the change between measuring light bundle and reference light bundle is brought about in that the two light sources are switched on alternately.
- each light beam is weakened by 50%. This leads to a deterioration in the signal-to-noise ratio, which can be critical for very sensitive measurements.
- DE-AS 1 964 469 is an atomic absorption
- Spectrometer known, in which the radiation emanates from a single radiation source designed as a line radiator, the radiation of which passes through the sample is frequency-modulated using the longitudinal Zeeman effect.
- a hollow cathode lamp sits between the pole pieces of an electromagnet.
- One of the pole pieces has a bore through which the measuring light beam passes.
- the measuring light beam then passes through a flame serving as an atomizing device and a monochromator and falls on a photoelectric detector.
- the electromagnet can be switched on and off, and the atomic absorption of the sample atoms, which is compensated for the background absorption, can be determined from the difference in the signals when the electromagnet is switched off and on.
- the windings of the electromagnet sit there on the pole shoes.
- the emission lines of the line-emitting light source are periodically shifted by the Zeeman effect and thus the emitted light is frequency-modulated and not the absorption lines of the sample.
- a spectral line is split into a central line, the wavelength of which corresponds to the undisplaced wavelength of the line in question when the magnetic field is switched off, and two side lines which are shifted towards higher and lower wavelengths.
- the central line and the side lines are polarized differently.
- the influence of the central line can therefore be eliminated by a polarizer.
- a polarizer results in 50% light loss.
- the invention has for its object to allow greater flexibility with regard to the determination of the background absorption in a device of the type mentioned and, depending on the existing conditions, to ensure working with an optimal signal level.
- this object is achieved in that (g) the beam splitter can optionally be moved out of the beam path.
- the full unattenuated measuring light bundle can also be used, whereby the reference light bundle is not reflected. If the background absorption does not change particularly quickly, it is then also possible to carry out the measurement of the background absorption using the Zeeman effect, without the beam of measurement being additionally weakened by a beam splitter. When the longitudinal Zeeman effect is used, there is no absorption line at the location of the original line, so that the light attenuation required by the transverse Zeeman effect is also eliminated by a polarizer.
- Embodiments of the invention are the subject of the dependent claims.
- the figure shows schematically the structure of an atomic absorption spectroether, in which the background absorption is compensated for by utilizing the longitudinal Zeeman effect.
- Preferred embodiment of the invention
- the figure is a schematic representation of the atomic absorption spectrometer.
- the atomic absorption spectrometer has a housing 10 in which the lamps, the optical system and the photosensitive detector are arranged.
- the housing 10 forms a sample space 12.
- An atomization device 14 is arranged in the sample space 12.
- the atomic absorption spectrometer has a hollow cathode lamp 16 as a first light source 16.
- the light source 16 emits a line spectrum that corresponds to the resonance lines of a specific, sought-after element.
- a measuring light bundle 18 extends from the light source 16.
- the measuring light beam 18 is deflected by a plane mirror 20 and collected by a concave mirror 22 through an opening 24 in the housing 10 in the middle of the sample space.
- the measuring light beam then passes through an opening 26 of the housing 10 aligned with the opening 24 and falls on a second concave mirror 28. From the second concave mirror 28, the measuring light beam 18 is focused via a plane mirror 30 on the entry slit 32 of a monochromator 34.
- a photoelectric detector 38 sits behind an exit gap 36 of the monochromator 34. The signal from the photoelectric detector 38 acts on a signal processing circuit 40.
- the atomization device 14 contains a furnace for electrothermal atomization, of which only the actual furnace body 42 is shown in FIG. 1, and an electromagnet 44 that can be switched on and off for generation of a magnetic field at the location of the sample.
- the electromagnet 44 has two aligned pole shoes 44 and 46, between which the furnace body 42 sits. Aligned bores 50 and 52 are provided in pole pieces 46 and 48. The bores 50 and 52 are aligned with a longitudinal bore 54 of the furnace body 42.
- the measuring light beam 18 runs through the bores 50 and 52 and through the longitudinal bore of the furnace body.
- Coil holders 56 and 58 are seated on pole pieces 50 and 52.
- Coils 60 and 62 of electromagnet 44 are wound on these coil holders 56 and 58.
- a power supply which controls the current through the furnace body 42. As indicated, the current is supplied transversely to the running direction of the measuring light bundle 18 and flows in the circumferential direction through the tubular furnace body 42.
- the electromagnet 44 is controlled by a magnetic control 66, such that the magnetic field is alternately switched on and off.
- the magnetic field of the electromagnet 44 extends at the location of the sample within the furnace body in the direction of travel of the measuring light beam 18.
- the longitudinal Zeeman effect is therefore generated on the sample atoms. This means that the absorption lines of the sample atoms are split into two lines, which are shifted relative to the undisturbed original absorption line.
- the atoms of the element sought no longer absorb the measuring light bundle 18, since this measuring light bundle only contains the unshifted resonance lines characteristic of the element.
- the portion of the real atomic absorption corrected for the background absorption can be determined from the measurements with the magnetic field switched on and off.
- the rhythm of the on and off circuit of the electromagnet 44 is for this purpose given to the signal evaluation circuit 40, as indicated by a line 68.
- a second light source 70 which emits a continuum, is seated in the housing 10.
- This second light source is a deuterium lamp.
- the second light source 70 emits a light bundle 72.
- This light bundle 72 from the second light source 70 can be pivoted into the beam path of the measurement beam 18 via a beam splitter 74 which can optionally be switched into the beam path.
- the first and the second light sources 16 and 70 can be switched on alternately in rapid succession, so that alternately a measurement light bundle 18 with a line spectrum from the first light source (hollow cathode lamp) 16 or a measurement light bundle with a continuum from the second light source (deuterium lamp) through the atomic cloud formed in the furnace body.
- the electromagnet is switched off.
- the background absorption can then be determined by alternately measuring the absorption of the very narrow spectral 1 inle of the first light source and the absorption of a band of continuum radiation which is wide relative to the spectral 1 and determined by the monochromator 34.
- the change between the first light source 16 and the second light source 70 takes place at a frequency of more than 500 Hertz, namely 1000 Hertz.
- Working with a second light source emitting a continuum as the reference light source makes it possible to detect relatively rapid changes in the background absorption which cannot be detected when the Zeeman effect is used by means of the electromagnet 44.
- the electromagnet 44 is relatively slow, so that the Frequency of the change between atomic absorption measurement and background measurement limits are set. By using the longitudinal Zeeman effect, no polarizer in the beam path is required. After the electromagnet has been switched off, the atomic absorption spectrometer can therefore work with a second light source 70 which emits a continuum, without double attenuation of light by a polarizer and additionally by the beam splitter 74.
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Abstract
Un spectromètre d'absorption atomique contient une première source lumineuse (16) émettant des lignes, et un système optique (20, 22, 28, 30, 34) pour créer un faisceau lumineux de mesure (18). Ce dernier passe à travers un espace d'échantillonnage (12) et heurte un détecteur photoélectrique (38). Un dispositif d'atomisation (14) est agencé dans l'espace d'échantillonnage pour l'atomisation d'un échantillon, de manière que les composantes de l'échantillon soient présentes sous forme atomique dans un espace d'atomisation traversé par le faisceau lumineux de mesure (18). Une seconde source de lumière (70) émettant un spectre continu est à l'origine d'un faisceau lumineux (72). Le faisceau lumineux de la seconde source lumineuse (70) est réfléchi par un fractionneur de rayons (74) sur la trajectoire des rayons du faisceau lumineux de mesure (18) et sert ainsi de faisceau lumineux de référence. Des moyens de branchement permettent de brancher les deux sources lumineuses (16, 70) alternativement. On peut, si on le souhaite, enlever le fractionneur de rayons (74) de la trajectoire des rayons. L'invention prévoit en outre un électro-aimant (44), qui crée un champ magnétique dans le sens du faisceau lumineux de mesure (18) là où se trouve l'échantillon atomisé et permet, facultativement, des mesures de fond spectral en vertu de l'effet Zeeman longitudinal.An atomic absorption spectrometer contains a first light source (16) emitting lines, and an optical system (20, 22, 28, 30, 34) for creating a measurement light beam (18). The latter passes through a sampling space (12) and collides with a photoelectric detector (38). An atomization device (14) is arranged in the sampling space for atomizing a sample, so that the components of the sample are present in atomic form in an atomization space crossed by the beam. measuring light (18). A second light source (70) emitting a continuous spectrum is the source of a light beam (72). The light beam of the second light source (70) is reflected by a ray splitter (74) on the path of the rays of the measurement light beam (18) and thus serves as a reference light beam. Connection means make it possible to connect the two light sources (16, 70) alternately. It is possible, if desired, to remove the beam splitter (74) from the beam path. The invention further provides an electromagnet (44), which creates a magnetic field in the direction of the measuring light beam (18) where the atomized sample is located and optionally allows spectral background measurements by virtue of of the longitudinal Zeeman effect.
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT89903130T ATE81404T1 (en) | 1988-03-18 | 1989-03-13 | ATOMIC ABSORPTION SPECTROMETER. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3809213 | 1988-03-18 | ||
DE3809213A DE3809213A1 (en) | 1988-03-18 | 1988-03-18 | ATOMIC ABSORPTION SPECTROMETER |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0404794A1 true EP0404794A1 (en) | 1991-01-02 |
EP0404794B1 EP0404794B1 (en) | 1992-10-07 |
Family
ID=6350143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89903130A Expired - Lifetime EP0404794B1 (en) | 1988-03-18 | 1989-03-13 | Atomic absorption spectrometer |
Country Status (6)
Country | Link |
---|---|
US (1) | US5181077A (en) |
EP (1) | EP0404794B1 (en) |
JP (1) | JP3047104B2 (en) |
AU (1) | AU624608B2 (en) |
DE (2) | DE3809213A1 (en) |
WO (1) | WO1989008832A1 (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3917955A1 (en) * | 1989-06-02 | 1990-12-06 | Bodenseewerk Perkin Elmer Co | DEVICE FOR ANALYZING MERCURY OR HYDRIDE IMAGES BY ATOMIC ABSORPTION MEASUREMENT |
JPH05215673A (en) * | 1992-01-31 | 1993-08-24 | Shimadzu Corp | Low-voltage discharge tube and atomic absorption spectrophotometer using same |
DE4230298C2 (en) * | 1992-09-10 | 2003-07-10 | Perkin Elmer Bodenseewerk Zwei | Atomic absorption spectrometer and high pressure lamp for an atomic absorption spectrometer |
EP0629851A3 (en) * | 1993-06-17 | 1995-03-22 | Fraunhofer Ges Forschung | Device for the analysis of traces of gas with absorption spectroscopy. |
DE4401745C2 (en) * | 1994-01-21 | 2003-02-06 | Perkin Elmer Bodenseewerk Zwei | Method for generating light for atomic absorption spectroscopy and atomic absorption spectroscopy system for carrying out the method |
DE4413096B4 (en) * | 1994-04-15 | 2004-09-09 | Berthold Gmbh & Co. Kg | Multi-element atomic absorption spectrometer and measuring method using such an atomic absorption spectrometer |
JPH0989763A (en) * | 1995-09-20 | 1997-04-04 | Hitachi Ltd | Atomic absorption spectrophotometer |
US5760895A (en) * | 1996-08-20 | 1998-06-02 | Aerodyne Research, Inc. | Optical monitor for water vapor concentration |
DE19635421C1 (en) * | 1996-08-23 | 1997-12-11 | Deutsche Forsch Luft Raumfahrt | Resonance absorption spectrometer for ion spectral analysis |
DE19740210B4 (en) * | 1997-09-12 | 2013-08-01 | PerkinElmer Singapore Pte.Ltd. | Atomic Absorption Spectrometer |
JP3508722B2 (en) * | 2000-12-25 | 2004-03-22 | 株式会社島津製作所 | Atomic absorption photometer |
WO2010094329A1 (en) * | 2009-02-19 | 2010-08-26 | Abb Research Ltd | Oxygen concentration measuring device and method for measuring oxygen |
CN102141518B (en) * | 2010-01-29 | 2013-04-10 | 上海华之光谱仪器有限公司 | Lorentz-force-free alternating current Zeeman background correction atomic absorption device and method |
CN102141509B (en) * | 2010-01-29 | 2012-10-24 | 上海华之光谱仪器有限公司 | Method for calculating and displaying background value of Zeeman background correction atomic absorption |
US9091590B2 (en) | 2011-12-28 | 2015-07-28 | Joseph Daniel Vance | Magneto-optic dispersion spectrometer |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5342797A (en) * | 1976-09-29 | 1978-04-18 | Seiko Instr & Electronics Ltd | Atomic absorption spectroscopic analyzer |
DE3113678A1 (en) * | 1981-04-04 | 1982-10-14 | Bodenseewerk Perkin-Elmer & Co GmbH, 7770 Überlingen | DEVICE FOR ATOMIC ABSORPTION ANALYSIS OF A SAMPLE |
JPS6057238A (en) * | 1983-09-09 | 1985-04-03 | Hitachi Ltd | Emission spectrometer |
JPS60187844A (en) * | 1984-03-07 | 1985-09-25 | Hitachi Ltd | Polarized Zeeman atomic absorption spectrophotometer |
JPS61231437A (en) * | 1985-04-08 | 1986-10-15 | Hitachi Ltd | Atomic absorption spectrophotometer |
-
1988
- 1988-03-18 DE DE3809213A patent/DE3809213A1/en not_active Withdrawn
-
1989
- 1989-03-13 US US07/549,013 patent/US5181077A/en not_active Expired - Lifetime
- 1989-03-13 WO PCT/EP1989/000260 patent/WO1989008832A1/en active IP Right Grant
- 1989-03-13 AU AU33521/89A patent/AU624608B2/en not_active Ceased
- 1989-03-13 EP EP89903130A patent/EP0404794B1/en not_active Expired - Lifetime
- 1989-03-13 DE DE8989903130T patent/DE58902429D1/en not_active Expired - Fee Related
- 1989-03-13 JP JP1502948A patent/JP3047104B2/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
---|
See references of WO8908832A1 * |
Also Published As
Publication number | Publication date |
---|---|
AU624608B2 (en) | 1992-06-18 |
AU3352189A (en) | 1989-10-05 |
EP0404794B1 (en) | 1992-10-07 |
DE58902429D1 (en) | 1992-11-12 |
JPH04501602A (en) | 1992-03-19 |
DE3809213A1 (en) | 1989-10-05 |
US5181077A (en) | 1993-01-19 |
WO1989008832A1 (en) | 1989-09-21 |
JP3047104B2 (en) | 2000-05-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2165106C2 (en) | Method and device for the analysis of atomic spectra | |
EP0404794A1 (en) | Atomic absorption spectrometer. | |
DE3119903A1 (en) | FLUORESCENCE SPECTROMETER | |
DE19511869A1 (en) | Process and arrangement for response analysis of semiconductor materials with optical excitation | |
DE4437575A1 (en) | Spectroscopy method using coherent, periodic radiation pulses aims two beams with different repetition frequencies | |
DE3886308T2 (en) | Spectrophotometer. | |
DE3215249C2 (en) | Photometer for measuring atomic fluorescence | |
DE3620324A1 (en) | METHOD AND DEVICE FOR ANALYZING ATOMIC SPECTRES | |
DE3886821T2 (en) | Voltage detector. | |
DE19636716C2 (en) | Atomic absorption spectrometer | |
DE3528300C2 (en) | ||
DE19740210B4 (en) | Atomic Absorption Spectrometer | |
DE3106441C2 (en) | Method for the quantitative determination of elements by Zeeman atomic absorption spectrometry and Zeeman atomic absorption spectrometer | |
DE3133894C2 (en) | Zeeman atomic absorption spectrometer | |
DE2854064C2 (en) | Method and device for measuring magneto-optic anisotropy | |
DE3782928T2 (en) | ATOMIC ABSORPTION SPECTRAL PHOTOMETER. | |
DD245491A1 (en) | PHASE-SENSITIVE FLUORESCENT DETECTOR FOR SHORT-TERM SPECTROSCOPY | |
DE10026280C2 (en) | Electro-optical scanning probe and measurement method using the probe | |
EP0215076A1 (en) | Absorption spectrometer with several successively activatable spectral light sources | |
DE102012202237B4 (en) | Apparatus and method for magnetic field measurement and control | |
DE3223334C2 (en) | Atomization unit for use in a Zeeman atomic absorption spectrometer, a forward scattering spectrometer or an atomic fluorescence spectrometer | |
DE19745607A1 (en) | Measurement of optical parameters of crystalline samples using reflected light | |
DD213512A1 (en) | FLUORESCENT DETECTOR FOR ROUTINE MEASUREMENTS IN SHORT-TERM SPECTROSCOPY | |
DD217024A1 (en) | Picosecond PHASENFLUOROMETER | |
AT260574B (en) | Device for measuring circular dichroism |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19900912 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE FR GB IT LI LU NL SE |
|
17Q | First examination report despatched |
Effective date: 19911011 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE FR GB IT LI LU NL SE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Effective date: 19921007 Ref country code: NL Effective date: 19921007 Ref country code: BE Effective date: 19921007 |
|
REF | Corresponds to: |
Ref document number: 81404 Country of ref document: AT Date of ref document: 19921015 Kind code of ref document: T |
|
REF | Corresponds to: |
Ref document number: 58902429 Country of ref document: DE Date of ref document: 19921112 |
|
ITF | It: translation for a ep patent filed | ||
GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) |
Effective date: 19930106 |
|
ET | Fr: translation filed | ||
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Effective date: 19930313 |
|
NLV1 | Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act | ||
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19930331 Ref country code: LI Effective date: 19930331 Ref country code: CH Effective date: 19930331 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20010302 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20010321 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20010426 Year of fee payment: 13 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020313 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20021001 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20020313 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20021129 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED. Effective date: 20050313 |